Literature DB >> 3231910

Autosomal dominant pattern dystrophy of the retinal pigment epithelium. Intrafamilial variability.

G Giuffrè1.   

Abstract

Three members of a family were affected by a pattern dystrophy of the retinal pigment epithelium transmitted by autosomal dominant inheritance. In addition to grossly impaired electro-oculograms and normal electroretinograms, the patients showed lesions of the fundus of the eye recalling those seen in Best's disease, multifocal Best's disease, and pattern dystrophies. The intrafamilial variability of the fundus lesions showed by this pattern dystrophy demonstrates the problems in the diagnosis of some dystrophies of this group.

Entities:  

Mesh:

Year:  1988        PMID: 3231910     DOI: 10.1097/00006982-198808030-00003

Source DB:  PubMed          Journal:  Retina        ISSN: 0275-004X            Impact factor:   4.256


  2 in total

1.  Butterfly-shaped pigment dystrophy of the fovea associated with subretinal neovascularization.

Authors:  F Marano; A F Deutman; A L Aandekerk
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1996-04       Impact factor: 3.117

2.  Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus.

Authors:  Camiel J F Boon; Mary J van Schooneveld; Anneke I den Hollander; Janneke J C van Lith-Verhoeven; Marijke N Zonneveld-Vrieling; Thomas Theelen; Frans P M Cremers; Carel B Hoyng; B Jeroen Klevering
Journal:  Br J Ophthalmol       Date:  2007-05-15       Impact factor: 4.638

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.